FDA 510(k) Applications Submitted by Kate Linak
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191742 | 07/01/2019 | ARIES MRSA Assay | Luminex Corporation |
| K163626 | 12/22/2016 | ARIES Bordetella Assay; ARIES Bordetella Assay Protocol File Kit | Luminex Corporation |
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